Stachydrine ameliorates high‐glucose induced endothelial cell senescence and SIRT1 downregulation. Issue 11 (13th September 2013)
- Record Type:
- Journal Article
- Title:
- Stachydrine ameliorates high‐glucose induced endothelial cell senescence and SIRT1 downregulation. Issue 11 (13th September 2013)
- Main Title:
- Stachydrine ameliorates high‐glucose induced endothelial cell senescence and SIRT1 downregulation
- Authors:
- Servillo, Luigi
D'Onofrio, Nunzia
Longobardi, Lara
Sirangelo, Ivana
Giovane, Alfonso
Cautela, Domenico
Castaldo, Domenico
Giordano, Antonio
Balestrieri, Maria Luisa - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb24598-sec-0001" sec-type="section"> <p>Hyperglycaemia, a characteristic feature of diabetes mellitus, induces endothelial dysfunction and vascular complications by accelerating endothelial cell (EC) senescence and limiting the proliferative potential of these cells. Here we aimed to investigate the effect of stachydrine, a proline betaine present in considerable quantities in juices from fruits of the <italic>Citrus</italic> genus, on EC under high‐glucose stimulation, and its underlying mechanism. The senescence model of EC was set up by treating cells with high‐glucose (30 mM) for different times. Dose‐dependent (0.001–1 mM) evaluation of cell viability revealed that stachydrine does not affect cell proliferation with a similar trend up to 72 h. Noticeable, stachydrine (0.1 mM) significantly attenuated the high‐glucose induced EC growth arrest and senescence. Indeed, co‐treatment with high‐glucose and stachydrine for 48 h kept the percentage of EC in the G<sub>0</sub>/G<sub>1</sub> cell cycle phase near to control values and significantly reduced cell senescence. Western blot analysis and confocal‐laser scanning microscopy revealed that stachydrine also blocked the high‐glucose induced upregulation of p16<sup>INK4A</sup> and downregulation of SIRT1 expression and enzyme activity. Taken together, results here presented are the first evidence that stachydrine, a naturally occurring compound<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb24598-sec-0001" sec-type="section"> <p>Hyperglycaemia, a characteristic feature of diabetes mellitus, induces endothelial dysfunction and vascular complications by accelerating endothelial cell (EC) senescence and limiting the proliferative potential of these cells. Here we aimed to investigate the effect of stachydrine, a proline betaine present in considerable quantities in juices from fruits of the <italic>Citrus</italic> genus, on EC under high‐glucose stimulation, and its underlying mechanism. The senescence model of EC was set up by treating cells with high‐glucose (30 mM) for different times. Dose‐dependent (0.001–1 mM) evaluation of cell viability revealed that stachydrine does not affect cell proliferation with a similar trend up to 72 h. Noticeable, stachydrine (0.1 mM) significantly attenuated the high‐glucose induced EC growth arrest and senescence. Indeed, co‐treatment with high‐glucose and stachydrine for 48 h kept the percentage of EC in the G<sub>0</sub>/G<sub>1</sub> cell cycle phase near to control values and significantly reduced cell senescence. Western blot analysis and confocal‐laser scanning microscopy revealed that stachydrine also blocked the high‐glucose induced upregulation of p16<sup>INK4A</sup> and downregulation of SIRT1 expression and enzyme activity. Taken together, results here presented are the first evidence that stachydrine, a naturally occurring compound abundant in citrus fruit juices, inhibits the deleterious effect of high‐glucose on EC and acts through the modulation of SIRT1 pathway. These results may open new prospective in the identification of stachydrine as an important component of healthier eating patterns in prevention of cardiovascular diseases. J. Cell. Biochem. 114: 2522–2530, 2013. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 114:Issue 11(2013:Nov.)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 114:Issue 11(2013:Nov.)
- Issue Display:
- Volume 114, Issue 11 (2013)
- Year:
- 2013
- Volume:
- 114
- Issue:
- 11
- Issue Sort Value:
- 2013-0114-0011-0000
- Page Start:
- 2522
- Page End:
- 2530
- Publication Date:
- 2013-09-13
- Subjects:
- Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.24598 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3294.xml